Lumbar Interbody Fusion
Keylink Composite Intervertebral Cage
Lumbar interbody fusion
Composite lumbar intervertebral cage combining PEEK and titanium-alloy technologies.
- Product type
- Composite intervertebral cage
- Application
- Lumbar interbody fusion
- Material / Platform
- Titanium alloy + PEEK composite design.
- Regulatory
- TFDA No. 008436
Product Overview
A composite lumbar interbody cage designed for L1-S1 fusion applications. The platform combines PEEK and titanium-alloy components in a single interbody construct.
Design & product features
Composite PEEK/titanium design
Lumbar interbody application
Multiple heights and lengths
Dedicated instrumentation
Models & Specifications
Available configurations within this product family. Refer to the current approved IFU and labeling for final model selection.
| Configuration | Details |
|---|---|
| 01 | Multiple model families |
| 02 | Lengths include 26, 28, 30 and 32 mm in the approved model tables |
| 03 | Multiple height options |
Sterility & processing
Gamma sterilized. The approved labeling specifies a 5-year shelf life.
Indications Overview
The points below summarize the approved product family. Final patient selection and surgical use must follow the applicable approved Instructions for Use.
- L1-S1 levels
- Lumbar degenerative disc disease
- Pseudarthrosis or failed spinal fusion
- Revision following disc-removal surgery
- Degenerative spondylolisthesis and Grade I spondylolisthesis
Product Visualization